HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249155Generated: October 29, 2026
Hydrochloric Acid → Benzyl 4-[3-(3-nitrobenzyl)indol-1-yl]-4-oxobutyrate
https://huagongshe.com/reaction/249155
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(3-Nitrobenzyl)indole | HCID 19024704 | — |
| Reactant | Benzyl phenyl succinate | HCID 19024784 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzyl 4-[3-(3-nitrobenzyl)indol-1-yl]-4-oxobutyrate | HCID 19024729 | 74.1% |
Reaction Steps
A solution of 3-(3-nitrobenzyl)indole (280 mg) in N,N-dimethylformamide (5 ml) was added to a suspension of sodium hydride (60% dispersion in mineral oil, 66.6 mg) in N,N-dimethylformamide (10 ml) at 0° C. The mixture was stirred at 25° C. for 40 minutes, and a solution of benzyl phenyl succinate (316 mg) in N,N-dimethylformamide was added at -40° C. After stirred at -40° C. for 20 minutes, the reaction mixture was poured into a mixture of ethyl acetate and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, and dried over, magnesium sulfate. After evaporation of the solvent, the crude crystals were washed with hot isopropyl ether to give benzyl 4-[3-(3-nitrobenzyl)indol-1-yl]-4-oxobutyrate (364 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212320 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-f987f97db3f54769b1057ea5e79dfa11 |
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| Source note | uspto-grants-1993_05 |
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